Mutations on the Protein: Q9UBX5 From Positions: 224 To 246
Swiss-Prot Disease: VAR_017153 
p.SER227PRO
N/A
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N/A
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Cutis laxa, autosomal recessive, 1A (ARCL1A)
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OMIM Disease: 604580.0001 
p.SER227PRO
N/A
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N/A
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CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA
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Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.
| DMDM_info@umbc.edu | 1000 Hilltop Circle, Baltimore, MD
21250 | Department of Biological Sciences | Phone: 410-455-2258 |
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